Genetics articles for University of Michigan (U-M), United States of America (USA)

Time frame: 1 June 2025 - 30 May 2026

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Count: 29

Article ‘Count’ for Genetics.

Journal Count Share
1 0.92
Non-Synaptic Function and Localization of Syntaxin-Binding Protein 1 in a Mouse Model of STXBP1-Related Epileptic Encephalopathy 0.92
1 0.02
DNA Methylation Signatures of Cardiovascular Health Provide Insights Into Diseases. 0.02
1 0.71
An X-to-autosome-to-Y chromosome amplified retrogene family functions in spermatids 0.71
1 0.80
Targeted delivery of rhodopsin’s assembled core is required for outer segment extension in mouse rod photoreceptors 0.80
3 0.17
Expanding the human proteome with microproteins and peptideins 0.06
CFAP20 salvages arrested RNAPII from the path of co-directional replisomes 0.04
CRISPR activation for SCN2A-related neurodevelopmental disorders 0.07
1 0.12
ER remodelling is a feature of ageing and depends on ER-phagy 0.12
11 4.66
Cytoplasmic localization of pseudouridine synthase 7 facilitates a pseudouridine-dependent enhancement of cellular stress tolerance 0.38
POMC neuron METTL14/m6A/YTHDC1/YTHDF2 pathways safeguard energy balance, body weight, and metabolism 0.75
A dual role of EZH2 in regulating A-to-I RNA editing and mRNA stability through ADAR 0.07
Co-transcriptional folding orchestrates sequential multi-effector sensing by a glycine tandem riboswitch 0.44
ALKB-1-dependent tRNA methylation is required for efficient paternal mitochondrial elimination 0.08
Repeatability of gene expression evolution in experimental environmental adaptation 1.00
Genetic architecture and mechanisms of host-microbiome interactions from a multi-cohort analysis of outbred laboratory rats 0.11
unctionally diversified Caenorhabditis elegans BiP orthologs control body growth, reproduction, stress resistance, aging, and autophagy 0.80
Epigenome-wide association study of nuclear DNA methylation in relation to mitochondrial heteroplasmy 0.16
linked myelination deficits and synaptic plasticity alterations drive auditory processing disorders in an ASD mouse model 0.60
A Hedgehog–Foxf axis coordinates dental follicle-derived alveolar bone formation 0.27
2 0.89
Pathogenic variants cause a neurodevelopmental syndrome by impairing synaptic function 0.01
Targeting histone H2B acetylated enhanceosomes via p300/CBP degradation in prostate cancer 0.89
2 1.30
A C. elegans model of copper deficiency: Dietary interventions rescue CTR1/CHCA-1 copper transporter mutant phenotype 0.30
Loss of FIC-1-mediated AMPylation activates the UPRER and upregulates cytosolic HSP70 chaperones to suppress polyglutamine toxicity 1.00
1 1.00
Rewarding touch limits lifespan through neural to intestinal signaling 1.00
3 2.92
Spontaneous mutation rate and spectrum are modulated by organismal fitness 1.00
Metabolic regulation of behavior by the intestinal enzyme FMO-2 1.00
Endogenous retrovirus-like proteins recruit UBQLN2 to stress granules and shape their functional biology 0.92
2 0.36
A leader-repeat hairpin blocks extraneous CRISPR RNA production in diverse CRISPR-Cas13 systems 0.25
The RNA m6A landscape during human oocyte-to-embryo transition. 0.11

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